Recuperation between 2 types of sedation after colonoscopy.

Phase 1

• Conditions: Ambulatory colonoscopy with sedation by target controlled infusion or manual titration of propofol.; MedDRA version: 19.0Level: LLTClassification code 10010010Term: Colonoscopy and sigmoidoscopy normalSystem Organ Class: 100000004848; Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

• Registration Number: EUCTR2014-005215-16-BE
• Lead Sponsor: CHU Brugmann

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-01-15
• Last Update Posted: 19 October 2020

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 160

Inclusion Criteria

All patients subjected to deep sedation in ambulant care
ASA status 1-3
18-80 years of age

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 90
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 70

Exclusion Criteria

Language barrier.
Dementia.
Gastroscopy planned at the same time.
Allergies to propofol.
All cases were a ‘full stomach’ is suspected (gastric banding)
Pregnancy.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified